HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235755Generated: October 30, 2026
Isopropanol → 2-[(2R, 3S)-3-(1-methoxy-1-methylethyl)-4-oxoazetidin-2-yl]acetic acid
https://huagongshe.com/reaction/235755
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | (3S, 4R)-4-(2-hydroxyethyl)-3-(1-methoxy-1-methylethyl)azetidin-2-one | HCID 56639466 | — |
| Reactant | Jones' reagent | HCID 131709961 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-[(2R, 3S)-3-(1-methoxy-1-methylethyl)-4-oxoazetidin-2-yl]acetic acid | HCID 56621919 | — |
Reaction Steps
A solution of (3S, 4R)-4-(2-hydroxyethyl)-3-(1-methoxy-1-methylethyl)azetidin-2-one (50.7 mg) in acetone (5.42 ml) was added to a solution of 2N Jones reagent (0.542 ml) in acetone (5.42 ml) at ambient temperature over a period of 30 minutes, and the mixture was stirred for an hour. After addition of an excess of isopropyl alcohol to the mixture, the solvent was removed. The residue was dissolved in chloroform and the resultant solution was washed with a saturated aqueous sodium chloride. The washings were extracted five times with chloroform. The extracts were combined, dried over magnesium sulfate, filtered and evaporated. The crystalline residue was washed with isopropyl alcohol to give 2-[(2R, 3S)-3-(1-methoxy-1-methylethyl)-4-oxoazetidin-2-yl]acetic acid (25.1 mg). The mother liquor was concentrated and the crystalline residue was washed with hexane to give a second crop of the above product (19.4 mg). Total yield is 44.5 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04640915 |
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| Source dataset | uspto-grants-1987_02 |
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| ORD ID | ord-80547e644c0d49b3bc4480657a38ecef |
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| Source note | uspto-grants-1987_02 |
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